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Psychotic episodes
Periods of time during which an individual experiences significant disturbances in their thoughts, perceptions, emotions, and behavior, resulting in a loss of touch with reality. These episodes are hallmark features of psychotic disorders such as schizophrenia, schizoaffective disorder, and certain forms of bipolar disorder.
Resumé
- Kropssystem
- Abnormality of the nervous system
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page$trait$nameLæs de gener, der er knyttet til Psychotic episodes, og resten af dit genom, med én test.
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Bestil min Genome Test27 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
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- Urea Cycle DisorderReads 2 of these genesSLC7A7NAGSAbout this report →
Show 23 more reports
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Læs de gener, der er knyttet til Psychotic episodes, og resten af dit genom, med én test.
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Bestil min Genome Test18 gener knyttet til Psychotic episodes
Ændringer i disse gener forårsager sjældne tilstande, hvor Psychotic episodes ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| MTHFRmethylenetetrahydrofolate reductase | Ofte (30–79 %) | I 1 tilstand |
| PITRM1pitrilysin metallopeptidase 1 | Ofte (30–79 %) | I 1 tilstand |
| ARMC5armadillo repeat containing 5 | Nogle gange (5–29 %) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Nogle gange (5–29 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| CDH23cadherin related 23 | Nogle gange (5–29 %) | I 1 tilstand |
| GNASGNAS complex locus | Nogle gange (5–29 %) | I 1 tilstand |
| KDM1Alysine demethylase 1A | Nogle gange (5–29 %) | I 1 tilstand |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PARK7Parkinsonism associated deglycase | Nogle gange (5–29 %) | I 1 tilstand |
| SLC7A7solute carrier family 7 member 7 | Nogle gange (5–29 %) | I 1 tilstand |
| TP53tumor protein p53 | Nogle gange (5–29 %) | I 1 tilstand |
| USP48ubiquitin specific peptidase 48 | Nogle gange (5–29 %) | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | Nogle gange (5–29 %) | I 1 tilstand |
| NAGSN-acetylglutamate synthase | Sjældent (1–4%) | I 1 tilstand |
| SNORD118small nucleolar RNA, C/D box 118 | Sjældent (1–4%) | I 1 tilstand |
| ATP13A2ATPase cation transporting 13A2 | Ikke registreret | I 1 tilstand |
| HMBShydroxymethylbilane synthase | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.21-311f020e.
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